Canonical Allele Identifier: CA2662662858

Gene: TMEM237

Linked Data

• gnomAD v4: 2-201640274-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201640274T>A , CM000664.2:g.201640274T>A	GRCh38
NC_000002.11:g.202504997T>A , CM000664.1:g.202504997T>A	GRCh37
NC_000002.10:g.202213242T>A	NCBI36
NG_032049.1:g.8256A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000621467.5:c.-356+619A>T	ENSP00000480508.2:n.-356+619A>T
ENST00000409883.7:c.75-9A>T MANE Select	ENSP00000386264.2:n.75-9A>T
ENST00000286196.9:c.-1+619A>T	ENSP00000286196.5:n.-1+619A>T
ENST00000409444.6:c.51-9A>T	ENSP00000387203.2:n.51-9A>T
ENST00000409883.6:c.75-9A>T	ENSP00000386264.2:n.75-9A>T
ENST00000432684.6:c.75-9A>T	ENSP00000413230.2:n.75-9A>T
ENST00000444047.6:c.75-9A>T	ENSP00000402681.2:n.75-9A>T
ENST00000463205.2:n.78-9A>T
ENST00000489550.5:n.92+619A>T
ENST00000621467.4:c.50+619A>T	ENSP00000480508.1:n.50+619A>T
NM_001044385.2:c.75-9A>T	NP_001037850.1:n.75-9A>T
NM_152388.3:c.51-9A>T	NP_689601.2:n.51-9A>T
NM_001044385.3:c.75-9A>T MANE Select	NP_001037850.1:n.75-9A>T
NM_152388.4:c.51-9A>T	NP_689601.2:n.51-9A>T